drugset / Trial / NCT02213887

Study of the Effects of Pantoprazole on Levels of Prescribed Psychiatric Medications

NCT02213887

Phase 4 Withdrawn University of British Columbia
Non-randomizedSingle-groupOpen-labelOther

Summary

The purpose of this 9-day study is to determine if: 1. Pantoprazole modifies the steady-state plasma concentrations of orally administered psychotropic medications including valproic acid, lithium, and second-generation antipsychotics (i.e., aripiprazole, asenapine, clozapine, lurasidone, olanzapine, paliperidone, quetiapine, risperidone, ziprasidone) 2. Serum gastrin levels change within a week of starting or stopping pantoprazole

Timeline

Start
2014-09
Primary completion
2020-11-02
Completion
2020-11-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Pantoprazole Other / unclassified 0 mg Oral
Subject Pantoprazole Other / unclassified 40 mg Oral